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FDA 510(k)

MODEL 580 DIGITAL RADIOGRAPHY SYSTEM

K-Number: K827501 · 1982-06-09

ApplicantTechnicare Corp.
Decision Date1982-06-09
Product Code
DecisionSubstantially Equivalent

Device Summary

MODEL 580 DIGITAL RADIOGRAPHY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Technicare Corp.. It received FDA 510(k) clearance on 1982-06-09 under 510(k) number K827501. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 580 DIGITAL RADIOGRAPHY SYSTEM?

MODEL 580 DIGITAL RADIOGRAPHY SYSTEM is a medical device that received FDA 510(k) clearance on 1982-06-09. The listed applicant is Technicare Corp.. The 510(k) number is K827501.

When did MODEL 580 DIGITAL RADIOGRAPHY SYSTEM receive FDA 510(k) clearance?

MODEL 580 DIGITAL RADIOGRAPHY SYSTEM received FDA 510(k) clearance on 1982-06-09, under 510(k) number K827501.

Who is the listed applicant for MODEL 580 DIGITAL RADIOGRAPHY SYSTEM?

The FDA 510(k) record lists Technicare Corp. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Technicare Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K854340TECHNICARE 720 HPS CT SCANNERK852089SATURN NUCLEAR MEDICINE COMPUTER SYSTEMK844293AUTO DII MULTI FREQUENCYK844247ULTRASONIC SCANNER CALIBRATION & TEST PHANTOMSK843716NUCLEAR 700 MEDICINE MECHANICAL POSIT-K842777AUTOFOCUS DUAL ELEMENT PROBE

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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